A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399907



Internal ID21057460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9604401..9606300hg38UCSC Ensembl
chr6:9604634..9606533hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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